267 related articles for article (PubMed ID: 10894222)
1. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families.
Kirby DM; Kahler SG; Freckmann ML; Reddihough D; Thorburn DR
Ann Neurol; 2000 Jul; 48(1):102-4. PubMed ID: 10894222
[TBL] [Abstract][Full Text] [Related]
2. [Leigh syndrome caused by the mitochondrial DNA G14459A mutation in a Mexican family].
Gutiérrez A; Saldaña-Martínez A; García-Ramírez R; Rayo-Mares D; Carreras M; López-Pérez MJ; Ruiz-Pesini E; Montoya J; Montiel-Sosa JF
Rev Neurol; 2009 Sep 1-15; 49(5):248-50. PubMed ID: 19714555
[TBL] [Abstract][Full Text] [Related]
3. Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.
Kirby DM; Boneh A; Chow CW; Ohtake A; Ryan MT; Thyagarajan D; Thorburn DR
Ann Neurol; 2003 Oct; 54(4):473-8. PubMed ID: 14520659
[TBL] [Abstract][Full Text] [Related]
4. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation.
Shoffner JM; Brown MD; Stugard C; Jun AS; Pollock S; Haas RH; Kaufman A; Koontz D; Kim Y; Graham JR
Ann Neurol; 1995 Aug; 38(2):163-9. PubMed ID: 7654063
[TBL] [Abstract][Full Text] [Related]
5. Leigh disease associated with a novel mitochondrial DNA ND5 mutation.
Taylor RW; Morris AA; Hutchinson M; Turnbull DM
Eur J Hum Genet; 2002 Feb; 10(2):141-4. PubMed ID: 11938446
[TBL] [Abstract][Full Text] [Related]
6. Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.
Funalot B; Reynier P; Vighetto A; Ranoux D; Bonnefont JP; Godinot C; Malthièry Y; Mas JL
Ann Neurol; 2002 Sep; 52(3):374-7. PubMed ID: 12205655
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
Kim JY; Hwang JM; Park SS
Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
[TBL] [Abstract][Full Text] [Related]
8. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
Lev D; Yanoov-Sharav M; Watemberg N; Leshinsky-Silver E; Lerman-Sagie T
Eur J Paediatr Neurol; 2002; 6(2):121-3. PubMed ID: 11995959
[TBL] [Abstract][Full Text] [Related]
9. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M
Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
[TBL] [Abstract][Full Text] [Related]
10. Leigh syndrome: clinical features and biochemical and DNA abnormalities.
Rahman S; Blok RB; Dahl HH; Danks DM; Kirby DM; Chow CW; Christodoulou J; Thorburn DR
Ann Neurol; 1996 Mar; 39(3):343-51. PubMed ID: 8602753
[TBL] [Abstract][Full Text] [Related]
11. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):129-31. PubMed ID: 11596342
[No Abstract] [Full Text] [Related]
12. [LHON (Leber's hereditary optic neuropathy)].
Mashima Y
Nihon Rinsho; 2002 Apr; 60 Suppl 4():282-6. PubMed ID: 12013866
[No Abstract] [Full Text] [Related]
13. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
[TBL] [Abstract][Full Text] [Related]
14. [A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].
Wei XQ; Kong QP; Zhang Y; Yang YL; Chang XZ; Qi Y; Qi ZY; Xiao JX; Qin J; Wu XR
Zhongguo Dang Dai Er Ke Za Zhi; 2009 May; 11(5):333-6. PubMed ID: 19470250
[TBL] [Abstract][Full Text] [Related]
15. The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome.
Santorelli FM; Shanske S; Macaya A; DeVivo DC; DiMauro S
Ann Neurol; 1993 Dec; 34(6):827-34. PubMed ID: 8250532
[TBL] [Abstract][Full Text] [Related]
16. [Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)].
Playán A; Solano-Palacios A; González de la Rosa JB; Merino-Arribas JM; Andreu AL; López-Pérez M; Montoya J
Rev Neurol; 2002 Jun 16-30; 34(12):1124-6. PubMed ID: 12134275
[TBL] [Abstract][Full Text] [Related]
17. Deficiency of respiratory chain complex I is a common cause of Leigh disease.
Morris AA; Leonard JV; Brown GK; Bidouki SK; Bindoff LA; Woodward CE; Harding AE; Lake BD; Harding BN; Farrell MA; Bell JE; Mirakhur M; Turnbull DM
Ann Neurol; 1996 Jul; 40(1):25-30. PubMed ID: 8687187
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications.
Makino M; Horai S; Goto Y; Nonaka I
J Hum Genet; 2000; 45(2):69-75. PubMed ID: 10721666
[TBL] [Abstract][Full Text] [Related]
19. Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene.
Budde SM; van den Heuvel LP; Janssen AJ; Smeets RJ; Buskens CA; DeMeirleir L; Van Coster R; Baethmann M; Voit T; Trijbels JM; Smeitink JA
Biochem Biophys Res Commun; 2000 Aug; 275(1):63-8. PubMed ID: 10944442
[TBL] [Abstract][Full Text] [Related]
20. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]